A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9908



Internal ID15539990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:91577332..91599805hg38UCSC Ensembl
Outerchr7:91206647..91229120hg19UCSC Ensembl
Outerchr7:91044583..91067056hg18UCSC Ensembl
Outerchr7:90851298..90873771hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3822474
hg1922474
hg1822474
hg1722474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835
Supporting Variants
SamplesNA18507
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv9908
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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